Open AccessFamiliar del3p syndrome: The uncertainty of the prognosis. A case report
Author(s) -
Martins Márcia,
Arantes Regina,
Botelho Pedro,
Souto Marta,
Moutinho Osvaldo,
Pinto Leite Rosário
Publication year - 2021
Publication title -
clinical case reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.21
H-Index - 9
ISSN - 2050-0904
DOI - 10.1002/ccr3.4036
Subject(s) - medicine , prenatal diagnosis , pediatrics , genetics , pregnancy , fetus , biology
The 3p deletion syndrome is an unusual condition. The few cases described are mainly de novo. We described a familial case detected in a prenatal diagnosis. Three members of the family had the 3p26.3‐p26.1 deletion; however, only the son presented clinical features.